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FDA 510(k)

RAD-X GLASSES

K-Number: K902280 · 1990-09-10

ApplicantCompudrug
Decision Date1990-09-10
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RAD-X GLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Compudrug. It received FDA 510(k) clearance on 1990-09-10 under 510(k) number K902280. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAD-X GLASSES?

RAD-X GLASSES is a medical device that received FDA 510(k) clearance on 1990-09-10. The listed applicant is Compudrug. The 510(k) number is K902280.

When did RAD-X GLASSES receive FDA 510(k) clearance?

RAD-X GLASSES received FDA 510(k) clearance on 1990-09-10, under 510(k) number K902280.

Who is the listed applicant for RAD-X GLASSES?

The FDA 510(k) record lists Compudrug as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RAD-X GLASSES?

The FDA product code for RAD-X GLASSES is HQY.

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Related Devices (Code: HQY)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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